化学
碲化镉光电
量子点
芯(光纤)
热液循环
壳体(结构)
类型(生物学)
纳米技术
光电子学
化学工程
光学
复合材料
物理
生物
工程类
生态学
材料科学
作者
Taichi Watanabe,K. Takahashi,Kunio Shimura,Hang‐Beom Bu,Kim Hyeon‐Deuk,DaeGwi Kim
标识
DOI:10.1246/bcsj.20160299
摘要
Abstract CdTe and CdTe/CdS quantum dots (QDs) were synthesized via hydrothermal method in one-step processes just by controlling reaction time. A gradual thermal decomposition of thiol ligand N-acetyl-l-cysteine results in formation of a CdS shell on a CdTe core. The experimental results of X-ray diffraction and energy dispersive X-ray spectroscopy indicated that growth of the CdS shell started in a longer reaction time than 30 minutes and that the thickness of the CdS shell increased with increasing the reaction time. The CdTe/CdS QD exhibited a longer photoluminescence-decay time than the CdTe core QD due to the type-II band alignment, and the decay time in the CdTe/CdS QDs increased with an increase in the reaction time. The increase in the decay time in the CdTe/CdS QDs was qualitatively reproduced by a decrease in an overlap integral of electron and hole wave functions caused by an increase of the CdS shell thickness.
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